A molecular recognition layer 21 is formed on a sensor face 6a of a chemical ccd 1 having such a structure that a plurality of potential wells 6 constituted to change a depth corresponding to a chemical quantity are arranged two-dimensionally, electric charges are injected into the potential wells 6, and the chemical quantity is converted into an electric charge corresponding to the sizes of the potential wells. Thus, it is provided a novel and useful molecular recognition type chemical ccd capable of measuring an ultramicro chemical substance with an ultrahigh sensitivity at a molecular level.
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1. A molecular recognition type chemical ccd comprising:
a chemical ccd having a plurality of potential wells constituted to change a depth corresponding to a chemical quantity, and being arranged two-dimensionally, in which electric charges are injected into the potential wells and the chemical quantity is converted into an electric charge corresponding to the sizes of the potential wells; a molecular recognition layer formed on a sensor face of a chemical ccd, said molecular recognition layer being structured to selectively capture molecular of certain chemical substances to allow the chemical ccd to output signals corresponding to the captured molecules.
2. The molecular recognition type chemical ccd according to
3. The molecular recognition type chemical ccd according to
4. The molecular recognition type chemical ccd according to any of
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The present invention relates to a molecular recognition type chemical charge coupled device (CCD) capable of measuring an ultramicro chemical substance with an ultrahigh sensitivity at a molecular level.
In recent years, it has been required that an environmental pollutant such as dioxin or environmental hormone and protein such as a DNA are measured at a ppb (parts per billion) or ppt (parts per tera) level. The environmental pollutant such as dioxin or environmental hormone should be measured by ultrahigh sensitivity analysis because an ultramicro substance is to be measured.
As a method of measuring ultramicro dioxin or environmental hormone, an SAW (surface acoustic wave) device method and a surface plasmon method have been studied. In the former method, an object to be measured is caused to come in contact with a surface elastic wave device and is measured based on a shift of a resonance frequency, which has a very high universality. It is apparent that analysis of 1 ng (nanogram), that is, in order of 1 ppb can be carried out with a frequency shift of 0.1 Hz. The latter method utilizes light transmission from the inside of an optical material to the outside. In any of the methods, the measurement can be carried out with a high sensitivity. However, an expensive device such as an electronic circuit or an optical system is required over the whole measuring system for operating the device.
For example, DNA measurement has been carried out in the following manner. More specifically, sections of approximately 10 mm square are formed on the surface of a slide glass. Hundreds to hundred thousands of fixed regions having a size of 10 μm2 including different probe DNAs from each other are arranged two-dimensionally in one section. One section acts as a DNA chip and has a size of 10 cm2. A chip surface is immersed in and washed with a solution containing a target DNA previously subjected to a labeling treatment with a fluorescent material, and the target DNA complementary to the probe DNA is hybridized (associated) to remain on a surface. The hybridized DNA chip surface can be measured as a fluorescent image through a fluorescent laser microscope and a CCD camera, and automatic control is carried out by a computer to perform a data processing. There has also been software in which genes to correspond to positions of a light emitting spot are previously registered in the computer, a fluorescent material for emitting green and red lights having a resolution of 1 to 10 μm is used to detect a feeble fluorescent intensity when forming a labeling piece, and hybridization profiles such as green and red signals or a yellow signal for double light emission can be compared in the same DNA chip.
However, the conventional method of measuring a DNA is based on a fluorescence method. The DNA to be measured is not directly measured. Therefore, there is a problem in that measuring precision basically depends on a conversion ratio. In addition, an expensive large-scale optical system is used. Therefore, there is a problem in that the whole device is expensive and large-sized.
In order to selectively and easily measure the object, a method of detecting a change in an electric potential of a functional substance as an ion selective electrode is the most effective. Examples of a method of directly and selectively measuring the substance to be measured include a mold polymerizing method (a molecular imprinting method). This method is also referred to as the mold polymerizing method in which a polymeric resin (host) and a substance to be measured (guest) are complexed and polymerized, and the guest is then removed to form a mold having a cavity in a portion of the host where the guest was present, and only molecules corresponding to the mold are taken out.
Examples of a method obtained by developing the mold polymerizing method include an interface mold polymerizing method. In the interface mold polymerizing method, a mold is formed on an oily water interface of a heterogeneous system in which a water layer and an oil layer are present together. The reaction to guest molecules does not reach the inside and is restricted to an interface. Therefore, there is an advantage that mass transfer is rapidly carried out and a response speed is higher than that of the ordinary mold polymerizing method.
In an electrochemical method, a change in a contact with environment pollution molecules can be directly taken as a signal. A large number of methods have been developed as a semiconductor sensor. In order to monitor an environmental polluting molecular concentration and to carry out remote sensing, the development of a gene manipulation technique of a microorganism and a useful function material is insufficient. For example, the remote sensing premises the field installation of an electronic device and plural sensing operations are required for real-time measurement.
There is a higher possibility that two-dimensional sensing might consequently obtain a new knowledge than the acquisition of an ultrahigh sensitivity of one sensor. According to simple calculation, it is possible to obtain a two-dimensional image signal including positional information in which face arrangement sensors of 4096, 16384 and 65536 correspond to a sensor in the two-dimensional sensing of 64×64, 128×128, and 256×256.
Furthermore, a technique for measuring bioimaging of molecules and cells has recently been developed remarkably. It is supposed that a device (chemical CCD) for transferring, through a CCD, electrochemical double layer surface charges generated on an interface between the environmental pollutant and the sensor will enable real-time two-dimensional chemical image measurement in the future. For the chemical CCD, it is proposed "Method and Apparatus for Measuring Physical Phenomenon or Chemical Phenomenon" in Japanese Patent Application No. Hei 9-157716 filed dated on May 29, 1997. The same has published as JP-A-10-332423 or EP-A-0881486. The structure and operation principle of the chemical CCD according to the patent application will be described below with reference to
In
A sensor section 13 is formed by each of the charge supply section 4, the charge injection adjusting section 5, the sensing section 6 and the barrier section 7. The sensing section 6 is formed of a potential well constituted to change a depth corresponding to a chemical quantity, which will be described below in detail. Moreover, an output section 14 is formed by each of the floating diffusion 9, the reset gate 10, the reset drain 11 and the output transistor 12.
As shown in
The principle of measurement of the chemical CCD 1 will be described below with reference to a potential diagram of FIG. 9. For the measurement, a pulse voltage is applied to the charge supply section 4, the barrier section 7 and the reset gate 10, while a DC voltage is applied to electrodes other than the floating diffusion 9.
In an ordinary MOS structure using a p-type semiconductor, there has been known the fact that a depletion layer is formed on an interface between an insulating film and a semiconductor depending on a positive voltage to be applied to a metal electrode. By using this phenomenon, a potential state is set in the vicinity of the interface of the semiconductor and the insulating film as shown in FIG. 9.
In a state 1, the electric potential of the charge supply section 4 is set to be high (in a direction of an arrow) and electric charges 15 are not injected into the sensing section 6 as shown in FIG. 9A.
In a state 2, the electric charges 15 are injected into the sensing section 6 by reducing the electric potential of the charge supply section 4 as shown in FIG. 9B.
In a state 3, electric charges 15a taken out by the charge injection adjusting section 5 are accumulated in the sensing section 6 by increasing the electric potential of the charge supply section 4 as shown in FIG. 9C.
In a state 4, the electric charges 15a accumulated in the sensing section 6 are transferred to the floating diffusion 9 by increasing the electric potential of the barrier section 7 as shown in FIG. 9D.
In a state 5, all the electric charges 15a of the sensing section 6 are transferred to the floating diffusion 9 to close the barrier section 7, thereby stopping the flow of the electric charges as shown in FIG. 9E. In this stage, the electric potential of the floating diffusion 9 is determined by the quantity of the electric charges 15a thus transferred. Therefore, the electric potential is input to a gate section of the output transistor 12 having the MOS structure, a drain current of the output transistor 12 is measured by a source follower circuit, for example, and the output is sent to a signal processor having a data processing function and an image processing function, for example, a computer (not shown).
In a state 6, the electric potential of the floating diffusion 9 is read and the reset gate 10 is then turned on to reset to the electric potential of the reset drain 11 as shown in FIG. 9F. By the resetting, the same state as the state 1 is returned again. In other words, the electric charges can be output to the outside by repeating the operations of the states 1 to 6.
As is understood from the description with reference to
The invention has been made in consideration of the foregoing and has an object to provide a novel and useful molecular recognition type chemical CCD capable of measuring an ultramicro chemical substance with an ultrahigh sensitivity at a molecular level.
In order to achieve the object, the invention provides a molecular recognition type chemical CCD in which a molecular recognition layer is formed on a sensor face of a chemical CCD having such a structure that a plurality of potential wells constituted to change a depth corresponding to a chemical quantity are arranged two-dimensionally, electric charges are injected into the potential wells, and the chemical quantity is converted into an electric charge corresponding to the sizes of the potential wells.
For example, in the case in which the molecular recognition layer is formed by a molecule imprinting method, concentrations of various chemical substances including an environment pollutant such as dioxin or environmental hormone can be measured with a high sensitivity at a molecular level. If the molecular recognition layer can individually recognize various kinds of chemical substances, they can be detected at the same time.
According to the third aspect of the invention, moreover, the molecular recognition layer is constituted by a DNA complementary to a DNA to be measured. Thus, the DNA to be measured can be detected with a high sensitivity.
According to the fourth aspect of the invention, in the case in which a gel having a solution containing a substance to be measured mixed into a gel material for migration is provided on an upper surface of the molecular recognition layer and a DC voltage is applied to the gel to measure the substance to be measured in the gel which is obtained after electrophoresis, the substance to be measured can be measured in a separation state.
An embodiment of the invention will be described with reference to the drawings.
In the molecule imprinting method, as shown in
As is typically shown in
According to the molecular recognition type chemical CCD 20 having such a structure, for example, when a very small quantity [for example, 1 nL (nanoliter)] of solution is dropped as a sample over the molecular recognition layer 21, a molecule of a chemical substance contained in the solution is recognized by the molecular recognizing section 22 formed corresponding to the molecule, and electric charges corresponding to the concentration of the chemical substance are output from the molecular recognizing section 22 and are taken out through the chemical CCD 1. Accordingly, the environmental pollutant such as dioxin or environmental hormone in the solution is simultaneously measured at a ppb or ppt level.
As described above, the molecular recognition type chemical CCD 20 according to the invention conforms to a surface potential measuring method on an electrode. Therefore, all charged substances can be measured by properly forming the molecular recognition layer 21.
While all the molecular recognizing sections 22 in the molecular recognition layer 21 may detect different chemical substances from each other, they may detect only a single chemical substance to measure two-dimensional distribution thereof.
Protein including a DNA can be measured by using the molecular recognition type chemical CCD 20 according to the first embodiment. In particular, the DNA can easily be measured by using the molecular recognition type chemical CCD having the following structure. A second embodiment will be described below.
In the molecular recognition type chemical CCD 20A having such a structure, it is possible to detect a DNA contained in a very small quantity of sample liquid which is put on the molecular recognition layer 31.
In the third embodiment, the molecular recognition layer may use the structure shown in
According to the molecular recognition type chemical CCD of the invention, the ultramicro chemical substance can be measured with an ultrahigh sensitivity at a molecular level. If the molecular recognition layer can individually recognize different kinds of chemical substances, a plurality of different chemical substances can be detected at the same time.
Patent | Priority | Assignee | Title |
7015963, | Jun 29 2001 | Horiba, LTD | CCD sensor incorporating parallel diffusion regions within the output |
7541610, | Jun 12 2006 | 3M Innovative Properties Company | LED device with re-emitting semiconductor construction and converging optical element |
7902542, | Jun 14 2006 | 3M Innovative Properties Company | Adapted LED device with re-emitting semiconductor construction |
7952110, | Jun 12 2006 | 3M Innovative Properties Company | LED device with re-emitting semiconductor construction and converging optical element |
7977660, | Aug 14 2007 | BL TECHNOLOGIES, INC | Article, device, and method |
Patent | Priority | Assignee | Title |
5164319, | Aug 22 1985 | MOLECULAR DEVICES, INC | Multiple chemically modulated capacitance determination |
5587273, | Jun 23 1994 | State of Oregon Acting by and Through the State Board of Higher Education on Behalf of the University of Oregon | Molecularly imprinted materials, method for their preparation and devices employing such materials |
6197503, | Nov 26 1997 | Lockheed Martin Energy Research Corporation | Integrated circuit biochip microsystem containing lens |
6203758, | Nov 10 1997 | Bio-Pixel Ltd. | Micro-circuit system with array of functionalized micro-electrodes |
DE4338732, | |||
EP881486, | |||
JP10332423, | |||
JP11201775, | |||
JP9236560, | |||
WO8707033, | |||
WO9627025, |
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